Regio- and stereoselective oxygenation of proline derivatives by using microbial 2-oxoglutarate-dependent dioxygenases

Biosci Biotechnol Biochem. 2014;78(8):1384-8. doi: 10.1080/09168451.2014.918490. Epub 2014 Jun 26.

Abstract

We evaluated the substrate specificities of four proline cis-selective hydroxylases toward the efficient synthesis of proline derivatives. In an initial evaluation, 15 proline-related compounds were investigated as substrates. In addition to l-proline and l-pipecolinic acid, we found that 3,4-dehydro-l-proline, l-azetidine-2-carboxylic acid, cis-3-hydroxy-l-proline, and l-thioproline were also oxygenated. Subsequently, the product structures were determined, revealing cis-3,4-epoxy-l-proline, cis-3-hydroxy-l-azetidine-2-carboxylic acid, and 2,3-cis-3,4-cis-3,4-dihydroxy-l-proline.

Keywords: dihydroxyproline; dioxygenase; hydroxylase; oxygenation; proline derivative.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Bacteria / enzymology*
  • Dioxygenases / metabolism*
  • Ketoglutaric Acids / metabolism*
  • Oxygen / chemistry*
  • Proline / analogs & derivatives*
  • Proline / chemistry*
  • Stereoisomerism
  • Substrate Specificity

Substances

  • Ketoglutaric Acids
  • Proline
  • Dioxygenases
  • Oxygen